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@karthikmbbs2
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Medical practitioner
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Location
Chennai
Website
kingofweapons.com
Created
2018-01-08 13:13
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karthikmbbs2
steemstem
8y
Leclanche cell
Leclanche cell A Leclanche cell consists of a carbon electrode packed in a porous pot containing manganese dioxide and charcoal powder. The porous pot is immersed in a saturated solution of ammonium chloride
$ 0.021
4
3
karthikmbbs2
steempress
8y
Majeed Syndrome
It is an inherited skin disorder characterized by chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and a neutrophilic dermatosis.[1] It is classified as an autoinflammatory
$ 0.000
1
karthikmbbs2
ardalanshojakiuru
8y
Ardalan–Shoja–Kiuru syndrome
Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin [1] amyloidosis and retinitis pigmentosa.[2] This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan
karthikmbbs2
anticonvulsantsulfonamide
8y
Anticonvulsant/sulfonamide hypersensitivity syndrome
Anticonvulsant/sulfonamide hypersensitivity syndrome is a potentially serious hypersensitivity reaction that can be seen with drugs with an aromatic amine chemical structure, such as aromatic anticonvulsants
karthikmbbs2
vincentb
8y
Amplified musculoskeletal pain syndromes
Amplified musculoskeletal pain syndromes are pain syndromes where excessive, acute and chronic pain are observed for which no overt primary cause can be found or surmised.[1] Amplified musculoskeletal
karthikmbbs2
thought
8y
Todays thought
Thanks for reading.. Have a great day..
karthikmbbs2
al-raqad
8y
Al-Raqad syndrome
Al-Raqad syndrome (ARS) is a congenital autosomal recessive syndrome discovered by Jordanian physician Mohammad Al-Raqad. It's characterized by: microcephaly growth delay Psycho-motor developmental delay
karthikmbbs2
aicardigoutires
8y
Aicardi–Goutières syndrome
Aicardi–Goutières syndrome (AGS), which is completely distinct from the similarly named Aicardi syndrome, is a rare, usually early onset childhood, inflammatory disorder most typically affecting the brain
karthikmbbs2
adie
8y
Adie syndrome
Adie syndrome is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodation (i.e., light-near dissociation).[1] It
karthikmbbs2
adamsnance
8y
Adams–Nance syndrome
Adams–Nance syndrome is a medical condition consisting of persistent tachycardia, paroxymal hypertension and seizures. It is associated with hyperglycinuria, dominantly inherited microphthalmia and cataracts.
karthikmbbs2
acute
8y
Acute motor axonal neuropathy
Acute motor axonal neuropathy (AMAN) is a variant of Guillain–Barré syndrome. It is characterized by acute paralysis and loss of reflexes without sensory loss. Pathologically, there is motor axonal
karthikmbbs2
acute
8y
Acute hepatomyoencephalopathy (HME) syndrome
Acute hepatomyoencephalopathy (HME) syndrome is the name given to a multi-system disease affecting the liver, muscle and brain which is now known to be caused by phytotoxins.[1] After extensive investigation
karthikmbbs2
acute
8y
acute chest syndrome
The acute chest syndrome is a vaso-occlusive crisis of the pulmonary vasculature commonly seen in people with sickle cell anemia. This condition commonly manifests with a new opacification of the lung(s)
karthikmbbs2
activation
8y
Activation syndrome
Activation syndrome is a form of stimulation (sometimes suicidal) or agitation that has been observed in association with some psychoactive drugs.[1] A causative role has not been established.[2] Pfizer
karthikmbbs2
acrodermatounguallacrimaltooth
8y
Acro–dermato–ungual–lacrimal–tooth (ADULT) syndrome
Acro–dermato–ungual–lacrimal–tooth (ADULT) syndrome is a rare genetic disease.[1] ADULT syndrome is an autosomal dominant form of ectodermal dysplasia, a group of disorders that affects the hair, teeth,
karthikmbbs2
ackerman
8y
Ackerman syndrome
Ackerman syndrome is a familial syndrome of fused molar roots with a single canal (taurodontism), hypotrichosis, full upper lip without a cupid’s bow, thickened and wide philtrum, and occasional juvenile
karthikmbbs2
achard
8y
Achard syndrome
Achard syndrome is a syndrome consisting of arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet.[1] Hypermobility and subluxations of the joints, increased lateral excursion
karthikmbbs2
ablepharon
8y
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome (AMS) is an extremely rare autosomal recessive genetic disorder characterized by malformations of the skull, skin, fingers and genitals.[1] Affected individuals may also
karthikmbbs2
abderhaldenkaufmannlignac
8y
Abderhalden–Kaufmann–Lignac syndrome
Abderhalden–Kaufmann–Lignac syndrome (AKL syndrome), also called nephropathic cystinosis, is an autosomal recessive renal disorder of childhood comprising cystinosis and renal rickets.
karthikmbbs2
abandoned
8y
Abandoned child syndrome
Abandoned child syndrome is a behavioral or psychological condition that results primarily from the loss of one or both parents, or sexual abuse. Abandonment may be physical (the parent is not present
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